Canonical Allele Identifier: CA352946087

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50345539-A-C
• MyVariant Identifiers: chr3:g.50382970A>C (hg19) ; chr3:g.50345539A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345539A>C , CM000665.2:g.50345539A>C	GRCh38
NC_000003.11:g.50382970A>C , CM000665.1:g.50382970A>C	GRCh37
NC_000003.10:g.50357974A>C	NCBI36
NG_023270.1:g.398T>G
NG_042828.1:g.5208T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.41T>G MANE Select	ENSP00000231749.3:p.Val14Gly
ENST00000231749.7:c.41T>G	ENSP00000231749.3:p.Val14Gly
ENST00000360165.7:c.41T>G	ENSP00000353289.3:p.Val14Gly
ENST00000431869.1:c.41T>G	ENSP00000391545.1:p.Val14Gly
ENST00000442887.1:c.-42T>G	ENSP00000393687.1:n.-42T>G
ENST00000443080.5:c.41T>G	ENSP00000415661.1:p.Val14Gly
ENST00000468182.1:n.143T>G
NM_001308379.1:c.41T>G	NP_001295308.1:p.Val14Gly
NM_015896.2:c.41T>G	NP_056980.2:p.Val14Gly
NM_015896.3:c.41T>G	NP_056980.2:p.Val14Gly
XM_005265216.2:c.-88T>G	XP_005265273.1:n.-88T>G
XM_005265216.3:c.-88T>G	XP_005265273.1:n.-88T>G
NM_015896.4:c.41T>G MANE Select	NP_056980.2:p.Val14Gly
NM_001308379.2:c.41T>G	NP_001295308.1:p.Val14Gly